Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
34,894 found- Lower riskFood
Ventura Foods, LLC recalls Sysco Imperial Glazed Hot Bacon Dressing; Net Contents 1 GAL; Distributed by Sysco Corporation, Houston, Texas 77077;
Ventura Foods recalls 1-gallon Imperial Glazed Hot Bacon Dressing due to plastic foreign object contamination. Consumers should check for lot date 11/29/2017 and contact Sysco for details.
Ventura FoodsDec 7, 2017 - Stop using nowConsumer product
Westinghouse Portable Generators Recalled by MWE Investments Due to Fire Hazard
Westinghouse iGen2500 and iPro2500 portable generators recalled due to overheating fire risk. Consumers must stop using and contact MWE Investments for free repair.
WestinghouseDec 7, 2017 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls Medtronic KYPHON(R) Express(TM) Directional Bone Filler Device, SIZE 2, REF FB, QTY 1 EA, Rx only STERILE R
Medtronic recalls specific size 2 directional bone filler devices due to potential misalignment of the directional arrow, which could lead to improper surgical placement. Affected units have unique lot numbers and are prescription-only.
MedtronicDec 6, 2017 - Use cautionMedical device
Reliance Medical Products Inc recalls Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to
Reliance Medical recalls Refractor Suspension Arms (P/N 525004, 05 and 525006, 07) due to missing washer, retaining ring, or stop screw that could cause falls during medical use.
Reliance MedicalDec 6, 2017 - Lower riskMedical device
Intel-GE Care Innovations LLC recalls Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a
Care Innovations recalls Health Harmony Mobile app version 2.5.2.29 due to delayed patient data syncing with clinicians, potentially causing missed medical information for up to two days.
Care InnovationsDec 6, 2017 - Use cautionVehicle
CAN-AM SPYDER RT (2017) recall — Exterior Lighting
BRP recalls 2017 Can-Am Spyder RT motorcycles with headlight beam too high on low setting, risking oncoming traffic blindness. Owners must have defective headlights replaced free by dealers.
Can-AmDec 5, 2017 - Use cautionVehicle
KEYSTONE RAPTOR (2018) recall — Structure
Keystone is recalling 2017-2018 Raptor fifth-wheel trailers with a risk of tire damage from outriggers, potentially causing loss of control. Owners must have a notch cut in the outriggers for safety.
KeystoneDec 5, 2017 - Use cautionMedical device
Ion Beam Applications S.A. recalls Proteus 235, Uniform and Pencil Beam Scanning The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and
Ion Beam Applications recalls Proteus 235 proton therapy systems due to risk of improper accessory insertion causing system operation without proper safety. Affected units may need verification and action.
Ion Beam ApplicationsDec 5, 2017 - Lower riskDrug
Sanofi-Aventis U.S. LLC recalls Enoxaparin Sodium, Injection 120 mg/0.8 mL, pre-filled, packaged in 10-count cartons, Rx Only, Winthrop US., a business
Sanofi recalls 10-count Enoxaparin Sodium injections with a labeling error that may cause incorrect dosing. Affected units have a syringe labeled 150 mg/1.0 mL in a blister pack marked 120 mg/mL.
SanofiDec 5, 2017 - Use cautionFood
Aldi Inc recalls Choceur Dark Chocolate Bars, 5.29 oz., 20 units/case
Aldi recalls Choceur Dark Chocolate Bars (5.29 oz, 20 units/case) due to undeclared almond pieces, a treenut allergen. Consumers should check best-by date (July 24, 2018).
AldiDec 5, 2017 - Use cautionFood
Creative Contract Packaging Corporation, LLC recalls HERB-OX Beef Flavor Granulated Bouillon, 4 ounce jars
Creative Contract Packaging recalls HERB-OX Beef Flavor Granulated Bouillon jars from Sept 2020 and Oct 2020 due to potential undeclared milk allergen. Consumers should check jar codes and contact for details.
Creative Contract PackagingDec 5, 2017 - Stop using nowConsumer product
Netgear Recalls Power Adapters for Outdoor Cameras Due to Fire Hazard
Netgear recalls the VMA4700 power adapter for Arlo cameras due to fire risk from water leakage. Stop using immediately and contact Netgear for a full refund.
NetgearDec 5, 2017 - Use cautionConsumer product
Metabo Recalls Rat Tail Angle Grinders Due to Laceration Hazard
Metabo recalls 5-7 inch rat tail angle grinders with brake due to laceration risk from on-off switch locking. Consumers must stop using and contact Metabo for free repair or replacement.
MetaboDec 5, 2017 - Lower riskMedical device
Life Technologies Corporation recalls Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UDI:
Life Technologies recalls Oncomine Dx Target Test User Guides and Assay Definition Files for non-small cell lung cancer tests. These may report incorrect results when used on samples other than NSCLC tumors.
Life TechnologiesDec 4, 2017 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in
Physio-Control
Physio-ControlDec 4, 2017 - UnratedMedical device
Accord Media, LLC recalls Ultra Renew Plus
Accord Media recalls Ultra Renew Plus devices due to unapproved green LED light used for hyperpigmentation treatment. Consumers should check if they own this device and follow official instructions.
Accord MediaDec 4, 2017 - Lower riskMedical device
Cellavision AB recalls CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the following products: CellaVision DM96, DM1200, DM9600
Cellavision AB recalls software versions 6.0.1 and 6.0.2 for DM96, DM1200, and DM9600 devices. These versions may not send WBC, RBC, and PLT data to lab systems when processing multiple slides per blood sample.
CellavisionDec 4, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls iChem VELOCITY Urine Chemistry Strips, REF 800-7212 Product Usage: The iChem VELOCITY automated urine chemistry system
Beckman Coulter recalls iChem VELOCITY Urine Chemistry Strips (Lot 7212154A) due to incorrect leukocyte pad causing false negative results. Affected users should contact for replacement.
Beckman CoulterDec 4, 2017 - Use cautionMedical device
Konica Minolta Medical Imaging USA, Inc. recalls Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR, UDI: 04560141941588
Konica Minolta recalls Sonimage HS1 ultrasound kit AC adapters with product number A8AR due to risk of circuit board breakage causing smoke emission. Affected units have specific serial numbers starting with 'A8AR-'.
Konica MinoltaDec 4, 2017 - Use cautionMedical device
Smiths Medical ASD Inc. recalls PORT-A-CATH II PS/Titan, Tray PAC II. Labeled as: a. VEN LP, PU, 2.6MM, UL, 8.5FR/INTRO (1/EA); b. DL, LP, PU, 2.2MM,
Smiths Medical recalls PORT-A-CATH II PS/Titan and Tray PAC II kits that may have incorrect 6Fr/6.5Fr introducers instead of 8.5Fr. This could cause improper catheter placement during medical procedures.
Smiths MedicalDec 4, 2017 - Lower riskDrug
ALLERGAN recalls Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine,
Allergan recalls 100-count Viokace tablets (NDC 58914-117-10) due to subpotent drug stability issues. This affects prescription-only enzyme supplements for pancreatic enzyme replacement.
AllerganDec 4, 2017 - Lower riskDrug
AuroMedics Pharma LLC recalls Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only, Manufactured in India for: AuroMedics
AuroMedics recalls Pantoprazole Sodium 40mg injection vials due to glass particles found in one lot. This poses a risk of injury from glass fragments if injected.
AuroMedicsDec 4, 2017 - Use cautionDrug
Solco Healtcare US LLC recalls Gabapentin Tablets, USP, 800 mg, 500-count, Rx only, Made in India, PONDRUGS/16 134193, Distributed by: Solco
Solco Healthcare recalls specific lots of Gabapentin 800mg tablets because bottles labeled as 800 mg may actually contain 600 mg.
Solco HealthcareDec 4, 2017 - Stop using nowFood
Premier Produce recalls Jicama Julienne, Brand Produce
Premier Produce recalls fresh cut Jicama Julienne contaminated with Listeria monocytogenes. Consumers should avoid eating this specific lot number.
Premier ProduceDec 4, 2017 - Lower riskFood
McCain Foods USA recalls Publix brand, item # 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's UPC # 0 41415 00549 5.
Publix recalls 32oz Southern Style Diced Hash Brown Potatoes due to foreign material complaints. Consumers should check product label for UPC 041415005495 and contact Publix for details.
PublixDec 4, 2017 - Stop using nowConsumer product
West Elm Recalls Table Lamps Due to Shock Hazard
West Elm recalls Industrial Task table lamps due to risk of electric shock from frayed electrical wires. Consumers must stop using and return lamps for full refund.
West ElmDec 4, 2017 - Lower riskMedical device
Fresenius Vial Sa recalls Volumat MC Agilia Volumetric Infusion Pump, Model No. Z021135, Software version 1.7. Product Usage - The Volumat MC
Fresenius Vial recalls Volumat MC Agilia Volumetric Infusion Pump model Z021135 software version 1.7 due to potential software malfunctions. Affected healthcare facilities must update software to prevent issues.
Fresenius VialDec 2, 2017 - Lower riskMedical device
ProSun International, LLC recalls Sundream 12 V tanning bed
ProSun recalls Sundream 12V tanning beds with model numbers starting SUN12VH1R... due to reduced maximum tanning time from 30 to 20 minutes. Consumers should check their serial numbers.
ProSunDec 2, 2017 - Lower riskMedical device
Cyberonics, Inc recalls VNS(R) Therapy Programmer, GMDN: 44077, Model 3000 v1.0.2.2 Intended Use/Indications: United States Indications for
Cyberonics recalls Model 3000 VNS Therapy Programmers with v1.0.2.2 software that were distributed before FDA approval. These devices may have been used without proper software validation.
CyberonicsDec 2, 2017 - Use cautionMeat & poultry
Caesar's Pasta, LLC Recalls Beef Meatball Products Due To Misbranding and Undeclared Allergens
USDA recalls 46,810 pounds of Caesar's Pasta meatballs for undeclared egg allergen. Consumers urged to stop using these products immediately.
Caesar's PastaDec 1, 2017
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.